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Melphalan 140 mg/m(2) or 200 mg/m(2) for autologous transplantation in myeloma: results from the Collaboration to Collect Autologous Transplant Outcomes in Lymphoma and Myeloma (CALM) study. A report by the EBMT Chronic Malignancies Working Party

Melphalan at a dose of 200 mg/m(2) is standard conditioning prior to autologous hematopoietic stem cell transplantation for multiple myeloma, but a dose of 140 mg/m(2) is often used in clinical practice in patients perceived to be at risk of excess toxicity. To determine whether melphalan 200 mg/m(2...

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Autores principales: Auner, Holger W., Iacobelli, Simona, Sbianchi, Giulia, Knol-Bout, Cora, Blaise, Didier, Russell, Nigel H., Apperley, Jane F., Pohlreich, David, Browne, Paul V., Kobbe, Guido, Isaksson, Cecilia, Lenhoff, Stig, Scheid, Christof, Touzeau, Cyrille, Jantunen, Esa, Anagnostopoulos, Achilles, Yakoub-Agha, Ibrahim, Tanase, Alina, Schaap, Nicolaas, Wiktor-Jedrzejczak, Wieslaw, Krejci, Marta, Schönland, Stefan O., Morris, Curly, Garderet, Laurent, Kröger, Nicolaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ferrata Storti Foundation 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830386/
https://www.ncbi.nlm.nih.gov/pubmed/29217776
http://dx.doi.org/10.3324/haematol.2017.181339
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author Auner, Holger W.
Iacobelli, Simona
Sbianchi, Giulia
Knol-Bout, Cora
Blaise, Didier
Russell, Nigel H.
Apperley, Jane F.
Pohlreich, David
Browne, Paul V.
Kobbe, Guido
Isaksson, Cecilia
Lenhoff, Stig
Scheid, Christof
Touzeau, Cyrille
Jantunen, Esa
Anagnostopoulos, Achilles
Yakoub-Agha, Ibrahim
Tanase, Alina
Schaap, Nicolaas
Wiktor-Jedrzejczak, Wieslaw
Krejci, Marta
Schönland, Stefan O.
Morris, Curly
Garderet, Laurent
Kröger, Nicolaus
author_facet Auner, Holger W.
Iacobelli, Simona
Sbianchi, Giulia
Knol-Bout, Cora
Blaise, Didier
Russell, Nigel H.
Apperley, Jane F.
Pohlreich, David
Browne, Paul V.
Kobbe, Guido
Isaksson, Cecilia
Lenhoff, Stig
Scheid, Christof
Touzeau, Cyrille
Jantunen, Esa
Anagnostopoulos, Achilles
Yakoub-Agha, Ibrahim
Tanase, Alina
Schaap, Nicolaas
Wiktor-Jedrzejczak, Wieslaw
Krejci, Marta
Schönland, Stefan O.
Morris, Curly
Garderet, Laurent
Kröger, Nicolaus
author_sort Auner, Holger W.
collection PubMed
description Melphalan at a dose of 200 mg/m(2) is standard conditioning prior to autologous hematopoietic stem cell transplantation for multiple myeloma, but a dose of 140 mg/m(2) is often used in clinical practice in patients perceived to be at risk of excess toxicity. To determine whether melphalan 200 mg/m(2) and melphalan 140 mg/m(2) are equally effective and tolerable in clinically relevant patient subgroups we analyzed 1964 first single autologous transplantation episodes using a series of Cox proportional-hazards models. Overall survival, progression-free survival, cumulative incidence of relapse, non-relapse mortality, hematopoietic recovery and second primary malignancy rates were not significantly different between the melphalan 140 mg/m(2) (n=245) and melphalan 200 mg/m(2) (n=1719) groups. Multivariable subgroup analysis showed that disease status at transplantation interacted with overall survival, progression-free survival, and cumulative incidence of relapse, with a significant advantage associated with melphalan 200 mg/m(2) in patients transplanted in less than partial response (adjusted hazard ratios for melphalan 200 mg/m(2) versus melphalan 140 mg/m(2): 0.5, 0.54, and 0.56). In contrast, transplantation in very good partial or complete response significantly favored melphalan 140 mg/m(2) for overall survival (adjusted hazard ratio: 2.02). Age, renal function, prior proteasome inhibitor treatment, gender, or Karnofsky score did not interact with overall/progression-free survival or relapse rate in the melphalan dose groups. There were no significant survival or relapse rate differences between melphalan 200 mg/m(2) and melphalan 140 mg/m(2) patients with high-risk or standard-risk chromosomal abnormalities. In conclusion, remission status at the time of transplantation may favor the use of melphalan 200 mg/m(2) or melphalan 140 mg/m(2) for key transplant outcomes (NCT01362972).
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spelling pubmed-58303862018-03-16 Melphalan 140 mg/m(2) or 200 mg/m(2) for autologous transplantation in myeloma: results from the Collaboration to Collect Autologous Transplant Outcomes in Lymphoma and Myeloma (CALM) study. A report by the EBMT Chronic Malignancies Working Party Auner, Holger W. Iacobelli, Simona Sbianchi, Giulia Knol-Bout, Cora Blaise, Didier Russell, Nigel H. Apperley, Jane F. Pohlreich, David Browne, Paul V. Kobbe, Guido Isaksson, Cecilia Lenhoff, Stig Scheid, Christof Touzeau, Cyrille Jantunen, Esa Anagnostopoulos, Achilles Yakoub-Agha, Ibrahim Tanase, Alina Schaap, Nicolaas Wiktor-Jedrzejczak, Wieslaw Krejci, Marta Schönland, Stefan O. Morris, Curly Garderet, Laurent Kröger, Nicolaus Haematologica Article Melphalan at a dose of 200 mg/m(2) is standard conditioning prior to autologous hematopoietic stem cell transplantation for multiple myeloma, but a dose of 140 mg/m(2) is often used in clinical practice in patients perceived to be at risk of excess toxicity. To determine whether melphalan 200 mg/m(2) and melphalan 140 mg/m(2) are equally effective and tolerable in clinically relevant patient subgroups we analyzed 1964 first single autologous transplantation episodes using a series of Cox proportional-hazards models. Overall survival, progression-free survival, cumulative incidence of relapse, non-relapse mortality, hematopoietic recovery and second primary malignancy rates were not significantly different between the melphalan 140 mg/m(2) (n=245) and melphalan 200 mg/m(2) (n=1719) groups. Multivariable subgroup analysis showed that disease status at transplantation interacted with overall survival, progression-free survival, and cumulative incidence of relapse, with a significant advantage associated with melphalan 200 mg/m(2) in patients transplanted in less than partial response (adjusted hazard ratios for melphalan 200 mg/m(2) versus melphalan 140 mg/m(2): 0.5, 0.54, and 0.56). In contrast, transplantation in very good partial or complete response significantly favored melphalan 140 mg/m(2) for overall survival (adjusted hazard ratio: 2.02). Age, renal function, prior proteasome inhibitor treatment, gender, or Karnofsky score did not interact with overall/progression-free survival or relapse rate in the melphalan dose groups. There were no significant survival or relapse rate differences between melphalan 200 mg/m(2) and melphalan 140 mg/m(2) patients with high-risk or standard-risk chromosomal abnormalities. In conclusion, remission status at the time of transplantation may favor the use of melphalan 200 mg/m(2) or melphalan 140 mg/m(2) for key transplant outcomes (NCT01362972). Ferrata Storti Foundation 2018-03 /pmc/articles/PMC5830386/ /pubmed/29217776 http://dx.doi.org/10.3324/haematol.2017.181339 Text en Copyright© 2018 Ferrata Storti Foundation Material published in Haematologica is covered by copyright. All rights are reserved to the Ferrata Storti Foundation. Use of published material is allowed under the following terms and conditions: https://creativecommons.org/licenses/by-nc/4.0/legalcode. Copies of published material are allowed for personal or internal use. Sharing published material for non-commercial purposes is subject to the following conditions: https://creativecommons.org/licenses/by-nc/4.0/legalcode, sect. 3. Reproducing and sharing published material for commercial purposes is not allowed without permission in writing from the publisher.
spellingShingle Article
Auner, Holger W.
Iacobelli, Simona
Sbianchi, Giulia
Knol-Bout, Cora
Blaise, Didier
Russell, Nigel H.
Apperley, Jane F.
Pohlreich, David
Browne, Paul V.
Kobbe, Guido
Isaksson, Cecilia
Lenhoff, Stig
Scheid, Christof
Touzeau, Cyrille
Jantunen, Esa
Anagnostopoulos, Achilles
Yakoub-Agha, Ibrahim
Tanase, Alina
Schaap, Nicolaas
Wiktor-Jedrzejczak, Wieslaw
Krejci, Marta
Schönland, Stefan O.
Morris, Curly
Garderet, Laurent
Kröger, Nicolaus
Melphalan 140 mg/m(2) or 200 mg/m(2) for autologous transplantation in myeloma: results from the Collaboration to Collect Autologous Transplant Outcomes in Lymphoma and Myeloma (CALM) study. A report by the EBMT Chronic Malignancies Working Party
title Melphalan 140 mg/m(2) or 200 mg/m(2) for autologous transplantation in myeloma: results from the Collaboration to Collect Autologous Transplant Outcomes in Lymphoma and Myeloma (CALM) study. A report by the EBMT Chronic Malignancies Working Party
title_full Melphalan 140 mg/m(2) or 200 mg/m(2) for autologous transplantation in myeloma: results from the Collaboration to Collect Autologous Transplant Outcomes in Lymphoma and Myeloma (CALM) study. A report by the EBMT Chronic Malignancies Working Party
title_fullStr Melphalan 140 mg/m(2) or 200 mg/m(2) for autologous transplantation in myeloma: results from the Collaboration to Collect Autologous Transplant Outcomes in Lymphoma and Myeloma (CALM) study. A report by the EBMT Chronic Malignancies Working Party
title_full_unstemmed Melphalan 140 mg/m(2) or 200 mg/m(2) for autologous transplantation in myeloma: results from the Collaboration to Collect Autologous Transplant Outcomes in Lymphoma and Myeloma (CALM) study. A report by the EBMT Chronic Malignancies Working Party
title_short Melphalan 140 mg/m(2) or 200 mg/m(2) for autologous transplantation in myeloma: results from the Collaboration to Collect Autologous Transplant Outcomes in Lymphoma and Myeloma (CALM) study. A report by the EBMT Chronic Malignancies Working Party
title_sort melphalan 140 mg/m(2) or 200 mg/m(2) for autologous transplantation in myeloma: results from the collaboration to collect autologous transplant outcomes in lymphoma and myeloma (calm) study. a report by the ebmt chronic malignancies working party
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830386/
https://www.ncbi.nlm.nih.gov/pubmed/29217776
http://dx.doi.org/10.3324/haematol.2017.181339
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